Clinical Research Coordinator 1 - JR29876-3800
- The University of Chicago Expired
- Chicago, Illinois
- Full Time
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Job Description
This job was posted by : For more
information, please see:
**Department**
BSD OBG - Lengyel Lab
**About the Department**
The Lengyel/Kenny laboratory is part of the Department of Obstetrics and
Gynecology/ Section of Gynecologic Oncology, studying the biology of
ovarian cancer. The laboratory has about 18 members that study ovarian
cancer biology. We use a variety of cutting-edge methods, including
spatial proteomics, spatial metabolomics, 3D organotypic cultures of
human tissue, spatiotemporal characterization of the immune system, and
stable-isotype tracing in patients. Bioinformatic support and access to
all Core facilities at the University of Chicago are available in the
laboratory.
Our translational research laboratory is in the Center for Integrated
Science, a research building on campus that houses 40 independent
research groups.
This at-will position is wholly or partially funded by contractual grant
funding which is renewed under provisions set by the grantor of the
contract. Employment will be contingent upon the continued receipt of
these grant funds and satisfactory job performance.
**Job Summary**
The job performs routine assignments related to the documentation and
reporting of basic clinical studies. Supports decisions that impact
clinical research conducted across the University.
The job performs routine assignments related to the documentation,
analysis, and reporting of research data. Provides input to support the
strategic, administrative, operational, and financial decisions that
impact clinical research conducted across the University.
The Ob/Gyn Lengyel Lab is looking for a Clinical Research
Coordinator/Analyst I to join its ovarian cancer research team.
Specifically, the Clinical Research Analyst I will provide input to
support the strategic, administrative, and operational support for
translational research. The Clinical Research Analyst I will perform
routine assignments related to the documentation, analysis, and
reporting of research data.
**Responsibilities**
- Performs various aspects of clinical research, such as collecting
and processing specimens, interviewing subjects, taking vital signs,
and contributing to the case report.
- Coordinates and may participate in quality assurance reviews
conducted by study sponsors, federal agencies, or specially
designated review groups.
- Analyzes study-related documentation, such as protocol worksheets,
procedural manuals, adverse event reports, institutional review
board documents, or progress reports.
- Responsible for all aspects of research projects involving patients
on IRBs.
- Organizes recruiting, consenting and scheduling research subjects.
- Oversees development and amendments of study protocols.
- Directs collection and analysis of bio specimens collected for
clinical trial.
- Works collaboratively with the team and collaborators.
- Develops data collection tools.
- Maintains and builds databases; maintains bio specimen storage.
- Provides general administrative supports including maintenance of
documentation.
- Writes and updates all protocols for specimen collection and
processing. Ensures compliance with institutional, state, and
federal regulatory policies, procedures, directives, and mandates.
- Processing and banking of bio specimens (serum, plasma, ascites,
tumor, benign tissues) and extraction of DNA.
- Assists with various professional, organizational, and operational
tasks under direct supervision.
- Uses knowledge of clinical studies to coordinate the collection of
analyzable clinical research data and/or samples.
- Performs other related work as needed.
**Minimum Qualifications**
**Education:**
Minimum requirements include a college or university degree in related
fi ld.
**Work Experience:**
Minimum requirements include knowledge and skills developed through
**Certifications:**
**\-\--**
**Preferred Qualifications**
**Education:**
- Bachelor\'s degree in field relevant to the research (e.g., biology,
cell biology, cancer biology).
**Experience:**
- Experience working in an Academic Medical Center.
- Experience supporting physicians/faculty.
- Experience supporting leadership positions.
**Preferred Competencies**
- Excellent written and oral communication.
- Organization.
- Problem-solving.
- Collaboration.
- Attention to detail.
- Able to work autonomously.
- Skills with a wide variety of digital collaboration tools (Zoom, MS
Teams, Slack, etc.).
- Proficiency with MS Office suite.
**Working Conditions**
- Ability to use a computer for extended periods.
**Application Documents**
Resume (re
information, please see:
**Department**
BSD OBG - Lengyel Lab
**About the Department**
The Lengyel/Kenny laboratory is part of the Department of Obstetrics and
Gynecology/ Section of Gynecologic Oncology, studying the biology of
ovarian cancer. The laboratory has about 18 members that study ovarian
cancer biology. We use a variety of cutting-edge methods, including
spatial proteomics, spatial metabolomics, 3D organotypic cultures of
human tissue, spatiotemporal characterization of the immune system, and
stable-isotype tracing in patients. Bioinformatic support and access to
all Core facilities at the University of Chicago are available in the
laboratory.
Our translational research laboratory is in the Center for Integrated
Science, a research building on campus that houses 40 independent
research groups.
This at-will position is wholly or partially funded by contractual grant
funding which is renewed under provisions set by the grantor of the
contract. Employment will be contingent upon the continued receipt of
these grant funds and satisfactory job performance.
**Job Summary**
The job performs routine assignments related to the documentation and
reporting of basic clinical studies. Supports decisions that impact
clinical research conducted across the University.
The job performs routine assignments related to the documentation,
analysis, and reporting of research data. Provides input to support the
strategic, administrative, operational, and financial decisions that
impact clinical research conducted across the University.
The Ob/Gyn Lengyel Lab is looking for a Clinical Research
Coordinator/Analyst I to join its ovarian cancer research team.
Specifically, the Clinical Research Analyst I will provide input to
support the strategic, administrative, and operational support for
translational research. The Clinical Research Analyst I will perform
routine assignments related to the documentation, analysis, and
reporting of research data.
**Responsibilities**
- Performs various aspects of clinical research, such as collecting
and processing specimens, interviewing subjects, taking vital signs,
and contributing to the case report.
- Coordinates and may participate in quality assurance reviews
conducted by study sponsors, federal agencies, or specially
designated review groups.
- Analyzes study-related documentation, such as protocol worksheets,
procedural manuals, adverse event reports, institutional review
board documents, or progress reports.
- Responsible for all aspects of research projects involving patients
on IRBs.
- Organizes recruiting, consenting and scheduling research subjects.
- Oversees development and amendments of study protocols.
- Directs collection and analysis of bio specimens collected for
clinical trial.
- Works collaboratively with the team and collaborators.
- Develops data collection tools.
- Maintains and builds databases; maintains bio specimen storage.
- Provides general administrative supports including maintenance of
documentation.
- Writes and updates all protocols for specimen collection and
processing. Ensures compliance with institutional, state, and
federal regulatory policies, procedures, directives, and mandates.
- Processing and banking of bio specimens (serum, plasma, ascites,
tumor, benign tissues) and extraction of DNA.
- Assists with various professional, organizational, and operational
tasks under direct supervision.
- Uses knowledge of clinical studies to coordinate the collection of
analyzable clinical research data and/or samples.
- Performs other related work as needed.
**Minimum Qualifications**
**Education:**
Minimum requirements include a college or university degree in related
fi ld.
**Work Experience:**
Minimum requirements include knowledge and skills developed through
**Certifications:**
**\-\--**
**Preferred Qualifications**
**Education:**
- Bachelor\'s degree in field relevant to the research (e.g., biology,
cell biology, cancer biology).
**Experience:**
- Experience working in an Academic Medical Center.
- Experience supporting physicians/faculty.
- Experience supporting leadership positions.
**Preferred Competencies**
- Excellent written and oral communication.
- Organization.
- Problem-solving.
- Collaboration.
- Attention to detail.
- Able to work autonomously.
- Skills with a wide variety of digital collaboration tools (Zoom, MS
Teams, Slack, etc.).
- Proficiency with MS Office suite.
**Working Conditions**
- Ability to use a computer for extended periods.
**Application Documents**
Resume (re
Similar Jobs
This job was posted by : For more
information, please see:
**Department**
BSD OBG - Lengyel Lab
**About the Department**
The Lengyel/Kenny laboratory is part of the Department of Obstetrics and
Gynecology/ Section of Gynecologic Oncology, studying the biology of
ovarian cancer. The laboratory has about 18 members that study ovarian
cancer biology. We use a variety of cutting-edge methods, including
spatial proteomics, spatial metabolomics, 3D organotypic cultures of
human tissue, spatiotemporal characterization of the immune system, and
stable-isotype tracing in patients. Bioinformatic support and access to
all Core facilities at the University of Chicago are available in the
laboratory.
Our translational research laboratory is in the Center for Integrated
Science, a research building on campus that houses 40 independent
research groups.
This at-will position is wholly or partially funded by contractual grant
funding which is renewed under provisions set by the grantor of the
contract. Employment will be contingent upon the continued receipt of
these grant funds and satisfactory job performance.
**Job Summary**
The job performs routine assignments related to the documentation and
reporting of basic clinical studies. Supports decisions that impact
clinical research conducted across the University.
The job performs routine assignments related to the documentation,
analysis, and reporting of research data. Provides input to support the
strategic, administrative, operational, and financial decisions that
impact clinical research conducted across the University.
The Ob/Gyn Lengyel Lab is looking for a Clinical Research
Coordinator/Analyst I to join its ovarian cancer research team.
Specifically, the Clinical Research Analyst I will provide input to
support the strategic, administrative, and operational support for
translational research. The Clinical Research Analyst I will perform
routine assignments related to the documentation, analysis, and
reporting of research data.
**Responsibilities**
- Performs various aspects of clinical research, such as collecting
and processing specimens, interviewing subjects, taking vital signs,
and contributing to the case report.
- Coordinates and may participate in quality assurance reviews
conducted by study sponsors, federal agencies, or specially
designated review groups.
- Analyzes study-related documentation, such as protocol worksheets,
procedural manuals, adverse event reports, institutional review
board documents, or progress reports.
- Responsible for all aspects of research projects involving patients
on IRBs.
- Organizes recruiting, consenting and scheduling research subjects.
- Oversees development and amendments of study protocols.
- Directs collection and analysis of bio specimens collected for
clinical trial.
- Works collaboratively with the team and collaborators.
- Develops data collection tools.
- Maintains and builds databases; maintains bio specimen storage.
- Provides general administrative supports including maintenance of
documentation.
- Writes and updates all protocols for specimen collection and
processing. Ensures compliance with institutional, state, and
federal regulatory policies, procedures, directives, and mandates.
- Processing and banking of bio specimens (serum, plasma, ascites,
tumor, benign tissues) and extraction of DNA.
- Assists with various professional, organizational, and operational
tasks under direct supervision.
- Uses knowledge of clinical studies to coordinate the collection of
analyzable clinical research data and/or samples.
- Performs other related work as needed.
**Minimum Qualifications**
**Education:**
Minimum requirements include a college or university degree in related
fi ld.
**Work Experience:**
Minimum requirements include knowledge and skills developed through
**Certifications:**
**\-\--**
**Preferred Qualifications**
**Education:**
- Bachelor\'s degree in field relevant to the research (e.g., biology,
cell biology, cancer biology).
**Experience:**
- Experience working in an Academic Medical Center.
- Experience supporting physicians/faculty.
- Experience supporting leadership positions.
**Preferred Competencies**
- Excellent written and oral communication.
- Organization.
- Problem-solving.
- Collaboration.
- Attention to detail.
- Able to work autonomously.
- Skills with a wide variety of digital collaboration tools (Zoom, MS
Teams, Slack, etc.).
- Proficiency with MS Office suite.
**Working Conditions**
- Ability to use a computer for extended periods.
**Application Documents**
Resume (re
information, please see:
**Department**
BSD OBG - Lengyel Lab
**About the Department**
The Lengyel/Kenny laboratory is part of the Department of Obstetrics and
Gynecology/ Section of Gynecologic Oncology, studying the biology of
ovarian cancer. The laboratory has about 18 members that study ovarian
cancer biology. We use a variety of cutting-edge methods, including
spatial proteomics, spatial metabolomics, 3D organotypic cultures of
human tissue, spatiotemporal characterization of the immune system, and
stable-isotype tracing in patients. Bioinformatic support and access to
all Core facilities at the University of Chicago are available in the
laboratory.
Our translational research laboratory is in the Center for Integrated
Science, a research building on campus that houses 40 independent
research groups.
This at-will position is wholly or partially funded by contractual grant
funding which is renewed under provisions set by the grantor of the
contract. Employment will be contingent upon the continued receipt of
these grant funds and satisfactory job performance.
**Job Summary**
The job performs routine assignments related to the documentation and
reporting of basic clinical studies. Supports decisions that impact
clinical research conducted across the University.
The job performs routine assignments related to the documentation,
analysis, and reporting of research data. Provides input to support the
strategic, administrative, operational, and financial decisions that
impact clinical research conducted across the University.
The Ob/Gyn Lengyel Lab is looking for a Clinical Research
Coordinator/Analyst I to join its ovarian cancer research team.
Specifically, the Clinical Research Analyst I will provide input to
support the strategic, administrative, and operational support for
translational research. The Clinical Research Analyst I will perform
routine assignments related to the documentation, analysis, and
reporting of research data.
**Responsibilities**
- Performs various aspects of clinical research, such as collecting
and processing specimens, interviewing subjects, taking vital signs,
and contributing to the case report.
- Coordinates and may participate in quality assurance reviews
conducted by study sponsors, federal agencies, or specially
designated review groups.
- Analyzes study-related documentation, such as protocol worksheets,
procedural manuals, adverse event reports, institutional review
board documents, or progress reports.
- Responsible for all aspects of research projects involving patients
on IRBs.
- Organizes recruiting, consenting and scheduling research subjects.
- Oversees development and amendments of study protocols.
- Directs collection and analysis of bio specimens collected for
clinical trial.
- Works collaboratively with the team and collaborators.
- Develops data collection tools.
- Maintains and builds databases; maintains bio specimen storage.
- Provides general administrative supports including maintenance of
documentation.
- Writes and updates all protocols for specimen collection and
processing. Ensures compliance with institutional, state, and
federal regulatory policies, procedures, directives, and mandates.
- Processing and banking of bio specimens (serum, plasma, ascites,
tumor, benign tissues) and extraction of DNA.
- Assists with various professional, organizational, and operational
tasks under direct supervision.
- Uses knowledge of clinical studies to coordinate the collection of
analyzable clinical research data and/or samples.
- Performs other related work as needed.
**Minimum Qualifications**
**Education:**
Minimum requirements include a college or university degree in related
fi ld.
**Work Experience:**
Minimum requirements include knowledge and skills developed through
**Certifications:**
**\-\--**
**Preferred Qualifications**
**Education:**
- Bachelor\'s degree in field relevant to the research (e.g., biology,
cell biology, cancer biology).
**Experience:**
- Experience working in an Academic Medical Center.
- Experience supporting physicians/faculty.
- Experience supporting leadership positions.
**Preferred Competencies**
- Excellent written and oral communication.
- Organization.
- Problem-solving.
- Collaboration.
- Attention to detail.
- Able to work autonomously.
- Skills with a wide variety of digital collaboration tools (Zoom, MS
Teams, Slack, etc.).
- Proficiency with MS Office suite.
**Working Conditions**
- Ability to use a computer for extended periods.
**Application Documents**
Resume (re
Job ID: 482534872
Originally Posted on: 6/24/2025
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